Education and Training
Note: Please keep certificates and dates of completion as you will need this information for your CPHS application.
CITI Training: Required Human Subjects Research Training for UC Berkeley Faculty, Staff, and Students
UC Berkeley faculty (with some exceptions), staff, and students engaged in human subjects research must complete either the biomedical or social-behavioral human research course, depending upon which is most germane to the research, through the online Collaborative Institutional Training Initiative (CITI). All study personnel must successfully complete the required CITI course(s) before CPHS will grant research approval or determination of exemption.
UC Berkeley offers many CITI elective/optional modules and courses as well. You are welcome to take any of these courses to enhance your human subjects research knowledge in such areas as public health, records based research, FDA-regulated research, FERPA, HIPAA, Good Clinical Practice, Conflicts of Interest, Export Compliance, undocumented status in human research, and international issues. For faculty who wish to incorporate a short human subjects research overview into their courses or seminars, OPHS has designed a group titled, “Essentials of Human Subjects Research.” Please note: this course does not fulfill the policy requirements referred to above.
For those who completed a CITI Human Research course at another institution
The user should contact CITI Program to transfer modules in common. The user will need to complete the UC Berkeley course by completing any outstanding modules as applicable.
UC Berkeley has now added the “COVID-19: Back to Campus (2020-2021), Remote Contact Tracing, Participating in Vaccine Research & Insights for Higher Ed Leaders” course to our curriculum and access completion information.
- You must have a CITI Program account to access the course. If you, as a learner, do not have a CITI Program account please follow these instructions to register.
- Here is how your learners can access the course:
- Visit CITI and log in to your account.
- Click on “View Courses” next to your institution’s name from your Main Menu page.
- Click on “Add a course” below the Learner Tools section.
- Locate the “COVID-19: Back to Campus (2020-2021), Remote Contact Tracing, Participating in Vaccine Research & Insights for Higher Ed Leaders” course (location may vary).
- Follow these steps to retrieve your Completion Record after you have completed the course.
- Human Subjects Training Requirements: UCB Investigator and UCB Research Personnel (flowchart)
- Working With Research Study Participants: An Overview (PowerPoint)
UC System IRB Memorandum of Understanding (MOU) Training Requirements
All UC Berkeley faculty, staff, and students who want to use the UC System Memorandum of Understanding to rely on another UC System institution’s IRB review must complete and pass the Collaborative Institutional Training Initiative (CITI) online training program module sequence most germane to their area of study. The exception to this rule is when the study is NIH-funded: legacy Principal Investigators may substitute the NIH online training created in 2008 (if taken before 1/1/2021) or the Human Research Protection Training offered by the HHS Office for Protection of Human Subjects (OHRP) (see below) for the CITI online training.
NIH-Funded Principal Investigators and Key Personnel
Principal Investigators and Key Personnel of NIH-funded research with human subjects are required by the NIH to complete training in the protection of human research participants. This requirement may be satisfied by completing the online CITI course, or legacy Principal Investigators have the option of completing the Human Research Protection Training offered by the HHS Office for Protection of Human Subjects (OHRP). All lessons must be completed in order to fulfill the training requirement. Users should be careful to save a copy of their completion record as OHRP does not maintain a database of completion records. The 2008 online NIH course: NIH Online Course - Protecting Human Research Participants (PHRP) is no longer updated or maintained. If this course was completed before 1/1/2021, it may fulfill NIH’s training requirement.
NIH Clinical Trials
Effective January 1, 2017, NIH expects all NIH-funded clinical investigators and clinical trial staff who are involved in the design, conduct, oversight, or management of clinical trials to be trained in Good Clinical Practice (GCP). Recipients of GCP training are expected to retain documentation of their training. GCP training should be refreshed at least every three years in order to stay up to date with regulations, standards, and guidelines.
This requirement must be satisfied by completing one of the following online CITI courses for Good Clinical Practice (GCP), most germane to the research in question:
- Group 1: Clinical Trials - FDA Focus - Investigators and/or Team Members
- Group 2: Clinical Trials - ICH Focus - Investigators and/or Team Members
- Group 3: Clinical Investigations of Devices - Investigators and/or Team Members
- GCP – Social and Behavioral Research Best Practices for Clinical Research
NSF-Funded Students and Postdocs Training Requirements
Students and postdocs supported by NSF funding to conduct human subjects research must complete the CITI Responsible Conduct of Research (RCR) course in addition to the CITI human research course (i.e., Group 2 social behavioral or Group 1 biomedical human research course). The RCR human subjects research course does NOT substitute for the CITI human subjects research course and vice versa. The RCR course certificate should be retained for the grant Principal Investigator’s records and should not be attached to the eProtocol application. See Responsible Conduct of Research (RCR) Training for additional information.
U.S. Department of Education (ED) Grant Applicants, Grantees, and Subgrantees
The following online course provides an overview of the key issues surrounding the protection of human subjects in ED-funded research as required in 34 CFR Part 97.
Training for Investigators Using Protected Health Information (PHI)
Investigators using protected health information (e.g. individually identifiable health information from the Tang Center, Human Resources Health Plan, Athletics and Recreational Sports, Optometry Clinic, or other covered entities outside of UC Berkeley) are subject to the requirements of the Health Insurance Portability and Accountability Act (HIPAA), and must complete HIPAA Research Training below and submit the completion certificate with their application before their CPHS protocol will be approved.
- HIPAA Research Training: Online Tutorial Assessment on Research Aspects of HIPAA
- This tutorial was developed by the UC San Diego Human Subjects Protection Program and has been made available to the UC research community.
OPHS Outreach Presentations
The Director of Research Subject Protection and/or OPHS staff conduct a graduate student workshop each spring, and make educational presentations at classes, seminars, and other venues throughout the year. The presentations cover the fundamentals of human subjects research requirements and the CPHS application process, but can be geared to the specific interests and needs of your group. If you are interested in scheduling OPHS staff to speak to your class or group, please send your request to OPHS at email@example.com. (Note: Fulfillment of such requests depends on OPHS workload/staff availability and other factors at the time.)